| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:19946974-19947245 | Common:4; Rare:97 | ||||
| chr3:20186204-20186367 | Common:1; Rare:44 | ||||
| chr3:21751097-21751415 | Common:4; Rare:103 | ||||
| chr3:23202924-23203188 | Common:1; Rare:95 | ||||
| chr3:23916880-23917177 | Rare:112 | ||||
| chr3:25428107-25428277 | Rare:33 | ||||
| chr3:25783383-25783646 | Common:2; Rare:83; Clinvar (benign):3 | ||||
| chr3:25789962-25790112 | Common:4; Rare:60 | ||||
| chr3:28348771-28349182 | Common:3; Rare:133 | ||||
| chr3:29280864-29281085 | Common:3; Rare:41 | ||||
| chr3:32106402-32106712 | Common:4; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32502779-32502910 | Rare:41 | ||||
| chr3:32570738-32570970 | Common:1; Rare:100 | ||||
| chr3:33277321-33277482 | Common:1; Rare:42 | ||||
| chr3:33798435-33798681 | Common:2; Rare:78 |